Cyclobenzaprine Hydrochloride 42708-0197-20

Package NDC

42708-0197-20

Manufacturer: Qpharma, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 31, 2017
Listing Expires: December 31, 2027
Application: ANDA208170

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Active Ingredients

Ingredient	Strength
Cyclobenzaprine Hydrochloride	5 mg/1

Drug Class

Centrally-mediated Muscle Relaxation [PE]Muscle Relaxant [EPC]

Selected Package

42708-0197-20Selected

20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-197-20)